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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349932Generated: October 30, 2026

Tetrahydrofuran → HCID 70141318, compound

https://huagongshe.com/reaction/349932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 86760427HCID 86760427—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductHCID 70141318HCID 7014131863%

Reaction Steps

A mixture of ethyl(1-[2-(4-benzyloxyphenyl)ethyl]-3-phenyl-1H-pyrazol-4-yl)acetate (800 mg), 5% palladium-carbon (1.50 g), tetrahydrofuran (20 ml), and ethanol (30 ml) was stirred for 3 hours at room temperature under a hydrogen atmosphere. After the palladium-carbon was removed by filtration, the filtrate was concentrated. The residue was subjected to silica gel column chromatography, and ethyl [1-[2-(4-hydroxyphenyl)ethyl]-3-phenyl-1H-pyrazol-4-yl]acetate (400 mg, yield: 63%) was obtained as an oily substance from the fraction eluted with ethyl acetate-hexane (1:4, volume ratio).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179823B1
Source datasetuspto-grants-2007_02
ORD IDord-d679461a91fe409087ad89727a35e122
Source noteuspto-grants-2007_02